iFlash HCG - FDA Registration IVDR-00787

Access comprehensive regulatory information for iFlash HCG in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00787 and manufactured by Shenzhen Yhlo Biotech Co., Ltd. Building 1, YHLO Biopark, Baolong 2nd Road, Baolong Subdistrict, Longgang District, 518116 Shenzhen, People's Republic of China in China. The device was registered on January 03, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Lifeline Diagnostics Supplies, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.